Microarray Analysis Products & Reviews

Microarrays, also known as biochips, are used for the detection and analysis of multiple genes, proteins, antibodies, or biomarkers on a single microchip. This can reveal information on protein or gene expression, single nucleotide polymorphism (SNP), copy number variation (CNV), epigenetics and patient health in clinical diagnostic tests. Discover a range of microarray scanners and prefabricated antibody, protein, RNA and DNA microarrays for your analysis or consider creating your own custom microarrays with a microarray printer. Find the best microarray products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.

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ECM Cell Adhesion Array Kit, colorimetric

Merck

The CHEMICON® ECM Cell Adhesion Array Kit (Colorimetric) provides an ECM Array microtiter plate with a colorimetric detection format, allowing for large-scale screening and quantitative comparison of multiple samples/cell lines. The kit is designed as a rapid (1-2 hours), cost effective, efficient method for characterization of cell adhesion.

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ECM Cell Adhesion Array Kit, fluorometric

Merck

The CHEMICON® ECM Cell Adhesion Array Kit (Fluorometric) provides an ECM Array microtiter plate with a homogenous fluorescence detection format, allowing for large-scale screening and quantitative comparison of multiple samples/cell lines. The kit is designed as a rapid (1-2 hours), cost effective, efficient method for characterization of cell adhesion

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Sure Blot® CHEMI™ Hybridization & Detection Kit

Merck

CHEMICON's Sure Blot® CHEMI™ Hybridization & Detection Kit is designed to provide high quality, non-radioactive detection of digoxigenin-labeled DNA probes hybridized to Sure Blot® Nylon Membrane. As an integrated hybridization and detection system, Sure Blot® CHEMI™ is quality controlled to produce high signal and low background. Comparable sensitivity to 32P is typically observed for single-copy gene detection. Sufficient re…

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DNA Ladder Detection Kit

Merck

Chemicon's Quick Apoptotic DNA Ladder Detection Kit provides a fast and easy means for detection of DNA fragmentation in apoptotic cells. Unlike other similar kits which require 1-2 days to finish the procedure, the new detection method requires less than 90 minutes to prepare DNA in a single tube, without the need for extraction or the use of columns. DNA fragmentation can be easily visualized by agarose gel electrophoreses.…

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Dextran Sulfate 50% Solution

Merck

Dextran Sulfate (MW 500,000) is used as an additive in probe hybridization solutions. Its presence accelerates the rate of hybridization by 10 fold. The addition of Dextran Sulfate favors the formation of probe networks, resulting in greater sensitivity during membrane-bound nucleic acid analysis. The product is supplied as a 50% (w/v) solution.

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Hybrisol® I Hybridization Solution, (50% Formamide, 6X SSC)

Merck

Hybrisol® Hybridization Solutions are pre-made, ready-to-use solutions optimized for sensitive single and multiple gene copy detection using membrane-based hybridization techniques. They are designed to give maximum signal and clean background for hybridizations performed on nylon and nitrocellulose membranes. Hybrisol® Solution contains 10% Dextran Sulfate, 1% SDS, 50% Formamide, 6X SSC, Sheared DNA, and Modified Denhardt's S…

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Custom CGH Microarrays

Agilent Technologies

The Agilent Custom CGH+SNP Microarray product line uses Agilent’s SurePrint technology to design and print user-defined CGH+SNP microarrays. Using Agilent’s eArray free application, users can design their own CGH+SNP microarrays to detect copy number changes and copy neutral aberrations, such as loss of heterozygosity (LOH) and uniparental disomy (UPD), on the same array.

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Custom CGH+SNP Microarrays

Agilent Technologies

The Agilent Custom CGH+SNP Microarray product line uses Agilent’s SurePrint technology to design and print user-defined CGH+SNP microarrays. Using Agilent’s eArray free application, users can design their own CGH+SNP microarrays to detect copy number changes and copy neutral aberrations, such as loss of heterozygosity (LOH) and uniparental disomy (UPD), on the same array.

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